Enhancing nanoscale viscoelasticity characterization in bimodal atomic force microscopy†

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Soft Matter Pub Date : 2024-09-02 DOI:10.1039/D4SM00671B
Casey Erin Adam, Alba Rosa Piacenti, Sarah L. Waters and Sonia Contera
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引用次数: 0

Abstract

Polymeric, soft, and biological materials exhibit viscoelasticity, which is a time dependent mechanical response to deformation. Material viscoelasticity emerges from the movement of a material's constituent molecules at the nano- and microscale in response to applied deformation. Therefore, viscoelastic properties depend on the speed at which a material is deformed. Recent technological advances, especially in atomic force microscopy (AFM), have provided tools to measure and map material viscoelasticity with nanoscale resolution. However, to obtain additional information about the viscoelastic behavior of a material from such measurements, theoretical grounding during data analysis is required. For example, commercially available bimodal AFM imaging maps two different viscoelastic properties of a sample, the storage modulus, E′, and loss tangent, tan δ, with each property being measured by a different resonance frequency of the AFM cantilever. While such techniques provide high resolution maps of E′ and tan δ, the different measurement frequencies make it difficult to calculate key viscoelastic properties of the sample such as: the model of viscoelasticity that describes the sample, the loss modulus, E′′, at either frequency, elasticity E, viscosity η, and characteristic response times τ. To overcome this difficulty, we present a new data analysis procedure derived from linear viscoelasticity theory. This procedure is applied and validated by performing amplitude modulation–frequency modulation (AM–FM) AFM, a commercially available bimodal imaging technique, on a styrene–butadiene rubber (SBR) with known mechanical behavior. The new analysis procedure correctly identified the type of viscoelasticity exhibited by the SBR and accurately calculated SBR E, η, and τ, providing a useful means of enhancing the amount of information gained about a sample's nanoscale viscoelastic properties from bimodal AFM measurements. Additionally, being derived from fundamental models of linear viscoelasticity, the procedure can be employed for any technique where different viscoelastic properties are measured at different and discrete frequencies with applied deformations in the linear viscoelastic regime of a sample.

Abstract Image

Abstract Image

在双模原子力显微镜中加强纳米级粘弹性表征
聚合材料、软材料和生物材料都具有粘弹性,这是一种随时间变化的变形机械响应。材料的粘弹性源于材料的组成分子在纳米和微米尺度上的运动,以应对施加的变形。因此,粘弹性取决于材料变形的速度。最近的技术进步,特别是原子力显微镜(AFM)技术的进步,提供了以纳米级分辨率测量和绘制材料粘弹性图的工具。然而,要从此类测量中获得有关材料粘弹性行为的更多信息,需要在数据分析过程中奠定理论基础。例如,市场上销售的双模原子力显微镜成像技术可以绘制出样品的两种不同粘弹特性图,即存储模量 E′和损耗正切值 tan δ,每种特性都是通过原子力显微镜悬臂的不同共振频率测量的。虽然这种技术能提供 E′ 和 tan δ 的高分辨率图,但不同的测量频率使得计算样品的关键粘弹性特性变得困难,例如:描述样品的粘弹性模型、任一频率下的损耗模量 E′′、弹性 E、粘度 η 和特征响应时间 τ。 为了克服这一困难,我们提出了一种从线性粘弹性理论中衍生出来的新数据分析程序。通过在具有已知机械行为的丁苯橡胶(SBR)上执行振幅调制-频率调制(AM-FM)原子力显微镜(一种市售的双模成像技术),应用并验证了这一程序。新的分析程序正确识别了丁苯橡胶的粘弹性类型,并准确计算出丁苯橡胶的E、η和τ,为提高从双模原子力显微镜测量中获得的有关样品纳米级粘弹性特性的信息量提供了有用的方法。此外,由于该程序源自线性粘弹性的基本模型,因此可用于在样品的线性粘弹性体系中以不同的离散频率测量不同粘弹性特性的任何技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Soft Matter
Soft Matter 工程技术-材料科学:综合
CiteScore
6.00
自引率
5.90%
发文量
891
审稿时长
1.9 months
期刊介绍: Where physics meets chemistry meets biology for fundamental soft matter research.
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